DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTER— 510(k) K850505

Substantially Equivalent

Parke-Davis Co.

FDA 510(k) clearance K850505 for DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTER, Substantially Equivalent on 1985-03-11. Applicant: Parke-Davis Co..

Clearance details

Applicant: Parke-Davis Co.
Product code: Code BSO
Advisory panel: Anesthesiology
Date received: 1985-02-08
Decision date: 1985-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, MI, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code BSO

product code BSO

Malfunction: 688
Total: 688

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.